[1]Herman TE, Siegel MJ. Apert syndrome with omphalocele[J]. J Perinatol, 2010, 30(10): 695-697.
[2]Soanca A, Dudea D, Gocan H, Roman A, Culic B. Oral manifestations in Apert syndrome: case presentation and a brief review of the literature[J]. Rom J Morphol Embryol, 2010, 51(3): 581584.
[3]Lolis MS, Bowe WP, Shalita AR. Acne and systemic disease[J]. Med Clin North Am, 2009, 93(6): 1161-1181.
[4]De D, Narang T, Kanwar AJ, Dogra S. Brachycephaly and syndactyly: Apert's syndrome[J]. Indian J Dermatol Venereol Leprol, 2008, 74(4):395-396.
[5]Slaney SF, Oldridge M, Hurst JA, Moriss-Kay GM, Hall CM, Poole MD, et al. Differential effects of FGFR2 mutations on syndactyly and cleft palate in Apert syndrome[J]. Am J Hum Genet, 1996, 58(5): 923-932.
[6]Holmes G, Rothschild G, Roy UB, Deng CX, Mansukhani A, Basilico C. Early onset of craniosynostosis in an Apert mouse model reveals critical features of this pathology[J]. Dev Biol, 2009, 328(2): 273-284.
[7]Weber B, Schwabegger AH, Vodopiutz J, Janecke AR,Forstner R,Steiner H. Prenatal diagnosis of apert syndrome with cloverleaf skull deformity using ultrasound, fetal magnetic resonance imaging and genetic analysis[J]. Fetal Diagn Ther, 2010, 27(1): 51-56.
[8]Esparza J, Hinojosa J, García-Recuero I, Romance A, Pascual B, Martínez de Aragón A. Surgical treatment of isolated and syndromic craniosynostosis. Results and complications in 283 consecutive cases[J].Neurocirugia (Astur), 2008, 19(6): 509-529.
[9]Gur I, Peled IJ, de Leon Falewski G, Meyer S. Rehabilitation aspects of Apert's syndrome[J]. Isr J Med Sci, 1984, 20(1): 50-54.